ECSP21036982A - DERIVATIVES OF AMINO TRIAZOLO QUINAZOLINE 9-SUBSTITUTED AS ANTAGONISTS OF THE ADENOSINE RECEPTOR, PHARMACEUTICAL COMPOSITIONS AND THEIR USE - Google Patents
DERIVATIVES OF AMINO TRIAZOLO QUINAZOLINE 9-SUBSTITUTED AS ANTAGONISTS OF THE ADENOSINE RECEPTOR, PHARMACEUTICAL COMPOSITIONS AND THEIR USEInfo
- Publication number
- ECSP21036982A ECSP21036982A ECSENADI202136982A ECDI202136982A ECSP21036982A EC SP21036982 A ECSP21036982 A EC SP21036982A EC SENADI202136982 A ECSENADI202136982 A EC SENADI202136982A EC DI202136982 A ECDI202136982 A EC DI202136982A EC SP21036982 A ECSP21036982 A EC SP21036982A
- Authority
- EC
- Ecuador
- Prior art keywords
- pharmaceutical compositions
- quinazoline
- antagonists
- substituted
- derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2818—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
En su gran cantidad de formas de realización, la presente invención proporciona determinados compuestos de amino triazolo quinazolina 9-sustituidos de la Fórmula estructural (I), que consta en el resumen de la memoria técnica, y sales de aquellos farmacéuticamente aceptables, en donde el anillo A, R1 y R2 son como se definen en la presente, composiciones farmacéuticas que comprenden uno o más de estos compuestos (solos o en combinación con uno o más agentes terapéuticamente activos diferentes), y métodos para su preparación y uso, solos o en combinación con otros agentes terapéuticos, como antagonistas de receptores A2a y/o A2b, y en el tratamiento de diversas enfermedades, afecciones o trastornos que están mediadas, al menos en parte, por el receptor de adenosina A2a y/o el receptor de adenosina A2b.In its large number of embodiments, the present invention provides certain 9-substituted amino triazolo quinazoline compounds of structural Formula (I), which is contained in the abstract of the technical specification, and salts of those pharmaceutically acceptable, wherein the Ring A, R1 and R2 are as defined herein, pharmaceutical compositions comprising one or more of these compounds (alone or in combination with one or more other therapeutically active agents), and methods for their preparation and use, alone or in combination with other therapeutic agents, such as A2a and / or A2b receptor antagonists, and in the treatment of various diseases, conditions or disorders that are mediated, at least in part, by the adenosine A2a receptor and / or the adenosine A2b receptor .
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862774077P | 2018-11-30 | 2018-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP21036982A true ECSP21036982A (en) | 2021-06-30 |
Family
ID=69005832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSENADI202136982A ECSP21036982A (en) | 2018-11-30 | 2021-05-25 | DERIVATIVES OF AMINO TRIAZOLO QUINAZOLINE 9-SUBSTITUTED AS ANTAGONISTS OF THE ADENOSINE RECEPTOR, PHARMACEUTICAL COMPOSITIONS AND THEIR USE |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US11312719B2 (en) |
| EP (1) | EP3886988A1 (en) |
| JP (1) | JP7241871B2 (en) |
| KR (1) | KR102653800B1 (en) |
| CN (1) | CN113329791A (en) |
| AR (1) | AR117164A1 (en) |
| AU (1) | AU2019385905B2 (en) |
| BR (1) | BR112021010427B1 (en) |
| CA (1) | CA3120862C (en) |
| CL (1) | CL2021001406A1 (en) |
| CO (1) | CO2021006888A2 (en) |
| CR (1) | CR20210271A (en) |
| DO (1) | DOP2021000104A (en) |
| EA (1) | EA202191498A1 (en) |
| EC (1) | ECSP21036982A (en) |
| IL (1) | IL283334A (en) |
| JO (2) | JOP20210117A1 (en) |
| MA (1) | MA54298A (en) |
| MX (1) | MX2021006329A (en) |
| NI (1) | NI202100043A (en) |
| PE (1) | PE20211768A1 (en) |
| PH (1) | PH12021551196A1 (en) |
| SG (1) | SG11202105180PA (en) |
| TW (1) | TW202039496A (en) |
| WO (1) | WO2020112700A1 (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101586617B1 (en) | 2007-06-18 | 2016-01-20 | 머크 샤프 앤 도메 비.브이. | Antibodies to human programmed death receptor PD-1 |
| US11466017B2 (en) | 2011-03-10 | 2022-10-11 | Board Of Regents, The University Of Texas System | Heterocyclic inhibitors of PTPN11 |
| JP7044375B2 (en) | 2016-05-31 | 2022-03-30 | ボード オブ リージェンツ,ザ ユニバーシティ オブ テキサス システム | Heterocyclic inhibitor of PTPN11 |
| JP7297871B2 (en) | 2018-05-02 | 2023-06-26 | ナビール ファーマ,インコーポレイティド | Substituted heterocyclic inhibitors of PTPN11 |
| WO2020033828A1 (en) | 2018-08-10 | 2020-02-13 | Board Of Regents, The University Of Texas System | 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer |
| WO2020106560A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| WO2020106558A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| AU2019389169A1 (en) | 2018-11-30 | 2021-06-17 | Comet Therapeutics, Inc. | Cyclic pantetheine derivatives and uses thereof |
| JP2022511778A (en) * | 2018-11-30 | 2022-02-01 | メルク・シャープ・アンド・ドーム・コーポレーション | 7-, 8- and 10-substituted aminotriazoloquinazoline derivatives, pharmaceutical compositions and their use as adenosine receptor antagonists |
| US20240076297A1 (en) * | 2020-07-24 | 2024-03-07 | Merck Sharp & Dohme Llc | Adenosine a2a and a2b receptor dual antagonists for immuno-oncology |
| EP4185296A4 (en) * | 2020-07-24 | 2025-03-05 | Merck Sharp & Dohme LLC | Adenosine a2a and a2b receptor dual antagonists for immuno-oncology |
| WO2023158626A1 (en) * | 2022-02-16 | 2023-08-24 | Merck Sharp & Dohme Llc | Adenosine receptor antagonists, pharmaceutical compositions and their use thereof |
| KR20250004779A (en) | 2022-04-13 | 2025-01-08 | 길리애드 사이언시즈, 인코포레이티드 | Combination therapy for treating TROP-2 expressing cancers |
| EP4626892A1 (en) * | 2022-11-29 | 2025-10-08 | Merck Sharp & Dohme LLC | Adenosine a2a and a2b receptor antagonists, pharmaceutical compositions and use thereof |
| WO2025137640A1 (en) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Azaspiro wrn inhibitors |
| CN120398919B (en) * | 2024-02-01 | 2026-04-07 | 福石生物科技(合肥)有限公司 | Spirocyclic derivatives as WRN inhibitors and their use |
Family Cites Families (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3957766A (en) | 1970-06-19 | 1976-05-18 | Boehringer Mannheim G.M.B.H. | Novel nitrofuran compounds and pharmaceutical compositions |
| DE2109577A1 (en) | 1971-03-01 | 1972-09-14 | Boehringer Mannheim Gmbh | Antimicrobial Nitrofuran Derivatives and Process for the Production of the Same |
| US4713383A (en) | 1984-10-01 | 1987-12-15 | Ciba-Geigy Corporation | Triazoloquinazoline compounds, and their methods of preparation, pharmaceutical compositions, and uses |
| GB9524395D0 (en) | 1995-11-29 | 1996-01-31 | Nickerson Biocem Ltd | Promoters |
| DE19629378A1 (en) | 1996-07-20 | 1998-01-29 | Boehringer Ingelheim Kg | New triazolopurines, process for their preparation and their use as medicaments |
| SI1283839T1 (en) | 2000-05-26 | 2005-08-31 | Schering Corp | |
| US6759759B2 (en) | 2000-08-29 | 2004-07-06 | Tamagawa Seiki Kabushiki Kaisha | Rotary contactless connector and non-rotary contactless connector |
| AR037243A1 (en) | 2001-10-15 | 2004-11-03 | Schering Corp | ADENOSINE RECEIVER ANTAGONISTS A2A, A5-AMINO-IMIDAZOLO- [4,3-E] -1,2,4-TRIAZOL- [1,5-C] PYRIMIDINE, PHARMACEUTICAL COMPOSITIONS AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT |
| US6916811B2 (en) | 2001-11-30 | 2005-07-12 | Schering Corporation | Adenosine A2a receptor antagonists |
| TW200300686A (en) | 2001-11-30 | 2003-06-16 | Schering Corp | Adenosine A2a receptor antagonists |
| PT1537878E (en) | 2002-07-03 | 2010-11-18 | Ono Pharmaceutical Co | IMMUNOPOTENTIAL COMPOSITIONS |
| AU2003272886A1 (en) | 2002-09-24 | 2004-04-19 | Kyowa Hakko Kogyo Co., Ltd. | (1,2,4)-TRIAZOLO(1,5-c)PYRIMIDINE DERIVATIVE |
| WO2004056875A1 (en) | 2002-12-23 | 2004-07-08 | Wyeth | Antibodies against pd-1 and uses therefor |
| WO2004072286A1 (en) | 2003-01-23 | 2004-08-26 | Ono Pharmaceutical Co., Ltd. | Substance specific to human pd-1 |
| WO2004092177A1 (en) | 2003-04-09 | 2004-10-28 | Biogen Idec Ma Inc. | Triazolopyrazines and methods of making and using the same |
| PT1678182E (en) | 2003-10-28 | 2007-04-30 | Schering Corp | Process for preparing substituted 5-amino-pyrazolo- [4,3-e]-1,2,4-triazolo [1,5-c]pyrimidines |
| JP2007513091A (en) | 2003-12-01 | 2007-05-24 | シェーリング コーポレイション | Process for the preparation of substituted 5-amino-pyrazolo- [4,3-e] -1,2,4-triazolo [1,5-c] pyrimidines |
| KR20060135901A (en) | 2004-04-21 | 2006-12-29 | 쉐링 코포레이션 | Pyrazolo- [4,3-e] -1,2,4-triazolo- [1,5-c] pyrimidine adenosine A2a receptor antagonist |
| US7472383B2 (en) | 2004-08-13 | 2008-12-30 | Sun Microsystems, Inc. | System and method for providing exceptional flow control in protected code through memory layers |
| EP1836205B1 (en) | 2004-12-21 | 2009-06-10 | Schering Corporation | PYRAZOLO[1,5-A]PYRIMIDINE ADENOSINE A2a RECEPTOR ANTAGONISTS |
| PL2161336T5 (en) | 2005-05-09 | 2017-10-31 | Ono Pharmaceutical Co | Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics |
| CA2612241C (en) | 2005-07-01 | 2018-11-06 | Medarex, Inc. | Human monoclonal antibodies to programmed death ligand 1 (pd-l1) |
| CA2622741A1 (en) | 2005-09-19 | 2007-03-29 | Schering Corporation | 2-heteroaryl-pyrazolo-[4, 3-e]-1, 2, 4-triazolo-[1,5-c]-pyrimidine as adenosine a2a receptor antagonists |
| PE20070521A1 (en) | 2005-09-23 | 2007-07-13 | Schering Corp | 7- [2- [4- (6-FLUORO-3-METHYL-1,2-BENZYSOXAZOL-5-IL) -1-PIPERAZINYL] ETHYL] -2- (1-PROPINYL) -7H-PIRAZOLE- [4, 3-E] - [1,2,4] -TRIAZOL- [1,5-C] -PYRIMIDIN-5-AMINE AS ANTAGONIST OF THE ADENOSINE A2a RECEPTOR |
| ATE457988T1 (en) | 2006-06-26 | 2010-03-15 | Schering Corp | A2A ADENOSINE RECEPTOR ANTAGONISTS |
| US7691869B2 (en) | 2007-03-30 | 2010-04-06 | King Pharmaceuticals Research And Development, Inc. | Pyrrolotriazolopyrimidine derivatives, pharmaceutical compositions containing them and methods of treating conditions and diseases mediated by the adenosine A2A receptor activity |
| HUP0700395A2 (en) | 2007-06-07 | 2009-03-02 | Sanofi Aventis | Substituted [1,2,4] triazolo [1,5-a] quinolines, process for their preparation, pharmaceutical compositions thereof, and intermediates |
| KR101586617B1 (en) | 2007-06-18 | 2016-01-20 | 머크 샤프 앤 도메 비.브이. | Antibodies to human programmed death receptor PD-1 |
| PE20091101A1 (en) | 2007-12-18 | 2009-07-26 | Pharminox Ltd | 3-SUBSTITUTED-4-OXO-3,4-DIHYDRO-IMIDAZO [5,1-d] [1,2,3,5-TETRACINE-8-CARBOXYL ACID AMIDES AND ITS USE |
| US8415353B2 (en) | 2008-03-04 | 2013-04-09 | Merck Sharp & Dohme Corp. | Amino-quinoxaline and amino-quinoline compounds for use as adenosine A2a receptor antagonists |
| US8168757B2 (en) | 2008-03-12 | 2012-05-01 | Merck Sharp & Dohme Corp. | PD-1 binding proteins |
| JP2012500652A (en) | 2008-08-25 | 2012-01-12 | アンプリミューン、インコーポレーテッド | Targeted costimulatory polypeptides and methods of use for treating cancer |
| PL2342226T3 (en) | 2008-09-26 | 2017-01-31 | Dana-Farber Cancer Institute, Inc. | Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses thereof |
| EP4209510B1 (en) | 2008-12-09 | 2024-01-31 | F. Hoffmann-La Roche AG | Anti-pd-l1 antibodies and their use to enhance t-cell function |
| EP2509983B1 (en) | 2009-11-16 | 2014-09-17 | Merck Sharp & Dohme Corp. | FUSED TRICYCLIC COMPOUNDS WITH ADENOSINE A2a RECEPTOR ANTAGONIST ACTIVITY |
| US20130017199A1 (en) | 2009-11-24 | 2013-01-17 | AMPLIMMUNE ,Inc. a corporation | Simultaneous inhibition of pd-l1/pd-l2 |
| WO2012135084A1 (en) | 2011-03-31 | 2012-10-04 | Merck Sharp & Dohme Corp. | METABOLITES OF 2-(FURAN-2-YL)-7-(2-(4-(4-(2-METHOXYETHOXY)PHENYL)PIPERAZIN-1-YL)ETHYL)-7H-PYRAZOLO[4,3-e][1,2,4]TRIAZOLO[1,5-c]PYRIMIDIN-5-AMINE AND THEIR UTILITY AS ADENOSINE A2a RECEPTOR ANTAGONISTS |
| EP2739358B1 (en) | 2011-08-01 | 2018-11-28 | F.Hoffmann-La Roche Ag | Methods of treating cancer using pd-1 axis binding antagonists and mek inhibitors |
| US8751477B2 (en) | 2012-10-05 | 2014-06-10 | Iac Search & Media, Inc. | Quality control system for providing results in response to queries |
| US9495379B2 (en) | 2012-10-08 | 2016-11-15 | Veritas Technologies Llc | Locality aware, two-level fingerprint caching |
| WO2014101113A1 (en) | 2012-12-28 | 2014-07-03 | Merck Sharp & Dohme Corp. | Piperazine-substituted 7-methoxy-[1,2,4]triazolo[1,5-c]quinazolin-5-amine compounds with a2a antagonist properties |
| WO2014101120A1 (en) | 2012-12-28 | 2014-07-03 | Merck Sharp & Dohme Corp. | Heterobicyclo-substituted-7-methoxy-[1,2,4]triazolo[1,5-c]quinazolin-5-amine compounds with a2a antagonist properties |
| WO2015027431A1 (en) | 2013-08-29 | 2015-03-05 | Merck Sharp & Dohme Corp. | 2,2-difluorodioxolo a2a receptor antagonists |
| JP6779204B2 (en) | 2014-11-18 | 2020-11-04 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | Aminopyrazine compound with A2A antagonist properties |
| EP3227299B1 (en) | 2014-12-04 | 2021-05-26 | Merck Sharp & Dohme Corp. | Formulation inhibiting effects of low acid environment |
| US10138212B2 (en) | 2015-02-06 | 2018-11-27 | Merck Sharp & Dohme Corp. | Aminoquinazoline compounds as A2A antagonist |
| EP3307067B1 (en) | 2015-06-11 | 2022-11-02 | Merck Sharp & Dohme LLC | Aminopyrazine compounds with a2a antagonist properties |
| US10207002B2 (en) | 2015-06-26 | 2019-02-19 | Merck Sharp & Dohme Corp. | Sustained release formulation and tablets prepared therefrom |
| WO2017008205A1 (en) | 2015-07-10 | 2017-01-19 | Merck Sharp & Dohme Corp. | Substituted aminoquinazoline compounds as a2a antagonist |
| TWI781136B (en) | 2017-01-20 | 2022-10-21 | 美商阿克思生物科學有限公司 | Azolo-pyrimidine for the treatment of cancer-related disorders |
| WO2018166493A1 (en) | 2017-03-16 | 2018-09-20 | 江苏恒瑞医药股份有限公司 | Heteroaryl[4,3-c]pyrimidine-5-amine derivative, preparation method therefor, and medical uses thereof |
| JP7065113B2 (en) | 2017-04-07 | 2022-05-11 | 南京明徳新薬研発有限公司 | [1,2,4] Triazolo [1,5-c] pyrimidine derivative as an A2A receptor inhibitor |
| US20200369665A1 (en) | 2017-06-30 | 2020-11-26 | Ryvu Therapeutics S.A. | Imidazo[1,2-a]pyrazine modulators of the adenosine a2a receptor |
| US11498923B2 (en) | 2017-12-13 | 2022-11-15 | Merck Sharp & Dohme Llc | Substituted imidazo[1,2-c]quinazolines as A2A antagonists |
| EP3810610A1 (en) | 2018-05-18 | 2021-04-28 | Incyte Corporation | Fused pyrimidine derivatives as a2a / a2b inhibitors |
| WO2020033828A1 (en) | 2018-08-10 | 2020-02-13 | Board Of Regents, The University Of Texas System | 6-(4-amino-3-methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-3-(2,3-dichlorophenyl)-2-methylpyrimidin-4(3h)-one derivatives and related compounds as ptpn11 (shp2) inhibitors for treating cancer |
| WO2020106558A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| WO2020106560A1 (en) | 2018-11-20 | 2020-05-28 | Merck Sharp & Dohme Corp. | Substituted amino triazolopyrimidine and amino triazolopyrazine adenosine receptor antagonists, pharmaceutical compositions and their use |
| PY1999867A (en) | 2018-11-30 | 2020-10-19 | Syngenta Crop Protection Ag | THIAZOLE DERIVATIVES MICROBIOCIDES |
| AR117200A1 (en) | 2018-11-30 | 2021-07-21 | Syngenta Participations Ag | THIAZOL DERIVATIVES MICROBIOCIDES |
| US10870663B2 (en) | 2018-11-30 | 2020-12-22 | Glaxosmithkline Intellectual Property Development Limited | Compounds useful in HIV therapy |
| JP2022511778A (en) | 2018-11-30 | 2022-02-01 | メルク・シャープ・アンド・ドーム・コーポレーション | 7-, 8- and 10-substituted aminotriazoloquinazoline derivatives, pharmaceutical compositions and their use as adenosine receptor antagonists |
-
2019
- 2019-11-26 CR CR20210271A patent/CR20210271A/en unknown
- 2019-11-26 AR ARP190103450A patent/AR117164A1/en not_active Application Discontinuation
- 2019-11-26 CA CA3120862A patent/CA3120862C/en active Active
- 2019-11-26 EA EA202191498A patent/EA202191498A1/en unknown
- 2019-11-26 AU AU2019385905A patent/AU2019385905B2/en active Active
- 2019-11-26 JO JOP/2021/0117A patent/JOP20210117A1/en unknown
- 2019-11-26 EP EP19827893.9A patent/EP3886988A1/en active Pending
- 2019-11-26 KR KR1020217019802A patent/KR102653800B1/en active Active
- 2019-11-26 WO PCT/US2019/063136 patent/WO2020112700A1/en not_active Ceased
- 2019-11-26 MX MX2021006329A patent/MX2021006329A/en unknown
- 2019-11-26 JO JOP/2021/0116A patent/JOP20210116A1/en unknown
- 2019-11-26 PE PE2021000757A patent/PE20211768A1/en unknown
- 2019-11-26 BR BR112021010427-5A patent/BR112021010427B1/en active IP Right Grant
- 2019-11-26 MA MA054298A patent/MA54298A/en unknown
- 2019-11-26 SG SG11202105180PA patent/SG11202105180PA/en unknown
- 2019-11-26 CN CN201980090487.8A patent/CN113329791A/en active Pending
- 2019-11-26 TW TW108142874A patent/TW202039496A/en unknown
- 2019-11-26 US US16/695,367 patent/US11312719B2/en active Active
- 2019-11-26 JP JP2021530114A patent/JP7241871B2/en active Active
-
2021
- 2021-05-20 IL IL283334A patent/IL283334A/en unknown
- 2021-05-24 NI NI202100043A patent/NI202100043A/en unknown
- 2021-05-25 PH PH12021551196A patent/PH12021551196A1/en unknown
- 2021-05-25 EC ECSENADI202136982A patent/ECSP21036982A/en unknown
- 2021-05-26 CO CONC2021/0006888A patent/CO2021006888A2/en unknown
- 2021-05-27 CL CL2021001406A patent/CL2021001406A1/en unknown
- 2021-05-27 DO DO2021000104A patent/DOP2021000104A/en unknown
-
2022
- 2022-03-31 US US17/657,515 patent/US12060357B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CL2021001406A1 (en) | 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use. | |
| MX2021005839A (en) | ANTAGONISTS OF THE ADENOSINE AMINOTRIAZOLOPYRIMIDINE AND AMINOTRIAZOLOPYRAMIDINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE. | |
| MX2021006012A (en) | 7-, 8-, and 10-SUBSTITUTED AMINO TRIAZOLO QUINAZOLINE DERIVATIVES AS ADENOSINE RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITIONS AND THEIR USE. | |
| CL2024000552A1 (en) | NLRP3 inhibitors | |
| CL2022003185A1 (en) | Midazopyrimidines and triazolopyrimidines as a2a/a2b inhibitors ((sol. div. 202002198) | |
| CL2019002150A1 (en) | Substituted 3-phenyl-4-amino-imidazo [4,5-c] pyridin-2-one and 7-phenyl-6-amino-purin-8-one derivatives, tyrosine kinase inhibitors, in particular bruton tyrosine kinase (btk ); compositions containing the compounds; and use for diseases such as cancer, autoimmune, inflammatory, and thromboembolic. (divisional request 201703073) | |
| NI201800033A (en) | DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3PYRIDYL] -1-ISOPROPYL-IMIDAZO [4, 5-C] QUINOLIN -2-ONA AS SELECTIVE MODULATORS OF THE KINASE OF MUTATED TELANGIECTASIA (ATM) FOR THE TREATMENT OF CANCER. | |
| DOP2016000281A (en) | IMIDAZO COMPOUNDS [4,5-C] QUINOLIN-2-ONA AND ITS USE TO TREAT CANCER | |
| CL2018001146A1 (en) | Imidazo [4,5-c] quinolin-2-one compounds and their use in cancer treatment | |
| CL2012000589A1 (en) | Compounds derived from pyrrolo pyridine carboxamides, jak2 inhibitors; pharmaceutical composition comprising them; use in the treatment of myeloproliferative diseases or cancer, such as polycythemia vera, essential thrombocytopenia, multiple myeloma, among others. | |
| ECSP10010034A (en) | 2-ANILINOPURIN-8-ONAS AS TTK / MPS1 INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISORDERS | |
| ECSP22022322A (en) | TRIAZOLOPYRIMIDINES AS A2A/A2B INHIBITORS | |
| CO2018004933A2 (en) | Imidazo [4,5-c] quinolin-2-one compounds and their use in cancer treatment | |
| BR112018005589A2 (en) | "Compound, pharmaceutically acceptable composition, and use of a compound" | |
| EA202192093A1 (en) | PYRAZOLOPYRIDINES AND TRIAZOLOPYRIDINES AS A2A / A2B INHIBITORS | |
| MX2020012058A (en) | TRIAZOLOPYRIMIDINE COMPOUNDS AND THEIR USE IN THE TREATMENT OF CANCER. | |
| MX2019011271A (en) | COMPOUNDS AND METHODS FOR THE TREATMENT OF PARASITIC DISEASES. | |
| CO2019010029A2 (en) | Deuterated imidazo [4,5-c] quinolin-2-one compounds and their use in the treatment of cancer | |
| MX2020007443A (en) | 2,4,6,7-TETRAHYDRO-PYRAZOLO[4,3-D]PYRIMIDIN-5-ONE DERIVATIVES AND RELATED COMPOUNDS AS C5A RECEPTOR MODULATORS FOR THE TREATMENT OF VASCULITIS AND INFLAMMATORY DISEASES. | |
| CO2018010951A2 (en) | Cinnolin-4-amine compounds and their use in cancer treatment | |
| AR121183A1 (en) | TREATMENT METHODS FOR LUPUS NEPHRITIS WITH INTERLEUKIN-17 ANTAGONISTS (IL-17) | |
| MX2018013969A (en) | Combination of pure 5-ht6 receptor antagonists with nmda receptor antagonist. | |
| CL2024000317A1 (en) | Cyclopentathiophenecarboxamide derivatives as platelet-activating factor receptor antagonists | |
| UY37084A (en) | INDANO DERIVATIVES AND THEIR USE IN THERAPIES | |
| ES3063880T3 (en) | Pyrrolo[1,2-b]-2-pyridazinone compounds as 5-ht4 receptor agonists |